Pure Global

“DIESSE” CHORUS TOXOPLASMA IgG - Taiwan Registration cb8b66c4937509758f6f39850539b64c

Access comprehensive regulatory information for “DIESSE” CHORUS TOXOPLASMA IgG in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cb8b66c4937509758f6f39850539b64c and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIESSE DIAGNOSTICA SENESE S.P.A., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
1 Competitors
1 Recent Registrations
cb8b66c4937509758f6f39850539b64c
Registration Details
Taiwan FDA Registration: cb8b66c4937509758f6f39850539b64c
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“DIESSE” CHORUS TOXOPLASMA IgG
TW: “迪雅仕” 可錄思 弓漿蟲IgG抗體試劑組
Risk Class 2
MD

Registration Details

cb8b66c4937509758f6f39850539b64c

Ministry of Health Medical Device Import No. 027887

DHA05602788705

Company Information

Product Details

This product is used with the Chorus system to quantitatively detect Toxoplasma IgG antibodies in human serum.

C Immunology and microbiology devices

C3780 Toxoplasma rodent serum reagent

Imported from abroad

Dates and Status

Oct 29, 2015

Oct 29, 2025

Companies Making Similar Products
Top companies providing products similar to "“DIESSE” CHORUS TOXOPLASMA IgG"